Variant #0000688228 (NC_000001.10:g.65243311G>T, NM_002227.2:c.*56934C>A (JAK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.65243311G>T
DNA change (hg38) -
Published as RAVER2(NM_001366165.1):c.322G>T (p.V108F)
ISCN -
DB-ID JAK1_000019
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JAK1 NM_002227.2 ?/. - c.*56934C>A r.(=) p.(=)
RAVER2 NM_018211.3 ?/. - c.322G>T r.(?) p.(Val108Phe)


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